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Vecuronium Bromide

NDC 25021-686 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerSagent Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA205390
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVECURONIUM BROMIDE (1 mg/mL)
Marketing started20240701
Package count1

External sources

Source: openFDA. Public-domain (CC0).